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ARROW ULTRA 8 INTRA-AORTIC BALLOON CATHETERS (IABS) 8FR 30CC AND 40CC UNIVERSAL

Page Type
Cleared 510(K)
510(k) Number
K000729
510(k) Type
Special
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
74 days
Submission Type
Summary

ARROW ULTRA 8 INTRA-AORTIC BALLOON CATHETERS (IABS) 8FR 30CC AND 40CC UNIVERSAL

Page Type
Cleared 510(K)
510(k) Number
K000729
510(k) Type
Special
Applicant
Arrow Intl., Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/19/2000
Days to Decision
74 days
Submission Type
Summary